Journal article
Synthesis of 3-(Alkylamino)-, 3-(Alkoxy)-, 3-(Aryloxy)-, 3-(Alkylthio)-, and 3-(Arylthio)-1,2,4-triazines by Using a Unified Route with 3-(Methylsulfonyl)-1,2,4-triazine
DH Shi, JR Harjani, RW Gable, JB Baell
European Journal of Organic Chemistry | WILEY-V C H VERLAG GMBH | Published : 2016
Abstract
In our attempts to synthesize 3-(alkylthio)- and 3-(alkoxy)-1,2,4-triazines without substituents at the 5- or 6-position, the synthesis of their anticipated precursor 3-(methylsulfonyl)-1,2,4 triazine was also optimized. The reactivity of 3-(methylsulfonyl)-1,2,4-triazine towards alkyl and aryl thiols, primary and secondary alkylamines, phenols, and alcohols was explored, and the reactions were optimized to maximize the isolation of the corresponding 3-substituted 1,2,4-triazine. Good yields were obtained for the products of the reactions with all of the aforementioned nucleophiles, with the exception of alcohols, by using alkali metal carbonates. Higher yields of 3-(alkoxy)-1,2,4-triazines ..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
D.-H. S. acknowledges the scholarship support received from the Jiangsu Government (JS-2013-349). The authors acknowledge the fellowship support from the National Health and Medical Research Council of Australia (JBB #1020411) and the research support (#1102147). This study was supported by the National Health and Medical Research Council through the Independent Research Institute Infrastructure Support Scheme (NHMRC IRIISS) grant 361646 and a Victorian State Government Operational Infrastructure Scheme grant.